Comparative floral structure and systematics in Ochnaceae s.l. (Ochnaceae,Quiinaceae and Medusagynaceae; Malpighiales)

Ochnaceae s.l. (Ochnaceae, Quiinaceae and Medusagynaceae), one of the well‐supported subclades of the large order Malpighiales retrieved so far in molecular phylogenetic studies, were comparatively studied with regard to floral structure using microtome section series and scanning electron microscopy (SEM). Floral morphology, anatomy and histology also strongly reflect this close relationship. Potential synapomorphies of the subclade include: flowers nectarless, sepals of different sizes within a flower, petals not retarded in development and forming the protective organs of advanced floral buds, petal aestivation contort, petals with three vascular traces, petals reflexed over the sepals and directed toward the pedicel, polystemony, anthers almost or completely basifixed, gynoecium often with more than five carpels, short gynophore present, styles separate for at least their uppermost part and radiating outwards, suction‐cup‐shaped stigmas, vasculature forming a dorsal band of bundles in the upper stylar region, gynoecium epidermis with large, radially elongate cells, ovules either weakly crassinucellar or incompletely tenuinucellar with an endothelium, abundance of tanniferous tissues and sclerenchyma in floral organs. The most strongly supported subclade of two of the three families in molecular analyses, Quiinaceae and Medusagynaceae, is also particularly well supported by floral structural features, including the presence of functionally and morphologically unisexual flowers, a massive thecal septum that persists after anther dehiscence, styles radiating outward from the ovary, two lateral ovules per carpel, positioned one above the other, conspicuous longitudinal ribs on the ovary wall at anthesis, and a ‘false endothelium’ on the nucellus at anthesis. Additionally, the group fits well in Malpighiales and further emphasizes the relationship of Malpighiales with Celastrales and Oxalidales, and thus the unity of the COM clade. © 2012 The Linnean Society of London, Botanical Journal of the Linnean Society, 2012, 170 , 299–392.     

16S mitochondrial sequences associate morphologically dissimilar males and females of the family Phoridae (Diptera)

The genus Phora (Diptera, Phoridae) includes more than 50 species widely distributed in temperate regions of Eurasia and Africa. Taxonomic identification of most species is based upon the morphology of the male hypopygium: hence for many species, including the type species of the genus, females are unknown. We used mitochondrial 16S ribosomal RNA sequences to match males with previously unidentified females from Phora atra , P. stictica , and P. holosericea . We then identified morphological characters that allow identification of females of P. atra and P. stictica without recourse to DNA sequencing. Our results show that small scale sequencing can aid in the development of taxonomic characters for use in the field to identify previously cryptic females. This iterative method of identifying populations genetically followed by re-examination of morphology should allow development of better keys for rapid identification of heretofore cryptic populations of insects. We also found that sequences from individual of P. holosericea from Cambridge, England and Malakhovka, Russia, were more similar to each other than to sequences from a conspecific fly also collected in Cambridge. This result suggests that there is previously un-suspected population structuring in this species.  © 2002 The Linnean Society of London, Biological Journal of the Linnean Society , 2002, 77 , 267–273.     

New taxa of Japanese and New Zealand Eurystomellidae (Phylum Bryozoa) and their phylogenetic relationships

As presently recognized, the small cheilostome bryozoan family Eurystomellidae (superfamily Catenicelloidea) comprises just two genera: Eurystomella Levinsen, 1909 , with three Recent species, and Selenariopsis Maplestone, 1913 ; with one Recent and two fossil species. Within Eurystomella sensu lato , colonies range from uni-/biserial to multiserial and the smooth gymnocystal frontal shields of zooids may be entire or have one to several large foramina. Here we describe seven new Recent species of encrusting eurystomellids from New Zealand and Japan. Including species of Selenariopsis , a cladistic analysis was carried out on 11 eurystomellid species and five outgroup species, the latter representing the families Cribrilinidae, Euthyroididae, Petalostegidae, and Catenicellidae. The results of the analysis support restricting Eurystomella to multiserial species with large frontal foramina, median suboral sutures, and basal pore-chambers. Two new genera, both with imperforate frontal shields and uniporous mural septula, are segregated from Eurystomella : uni-/biserial Zygopalme , with a median suboral suture and accssory perforations in the ovicellular kenozooid, and multiserial Integripelta , lacking the suture and accessory perforations.  © 2002 The Linnean Society of London, Zoological Journal of the Linnean Society , 2002, 136 , 199–216.     

Small subunit rDNA and Bayesian inference reveal Pectenophilus ornatus (Copepoda incertae sedis) as highly transformed Mytilicolidae, and support assignment of Chondracanthidae and Xarifiidae to Lichomolgoidea (Cyclopoida)

Phylogenetic analysis of newly obtained data from the complete small subunit rDNA (18S) nuclear gene of a wide range of copepods placed the enigmatic Pectenophilus ornatus firmly in the Cyclopoida. Both maximum parsimony tree reconstruction, and Bayesian analysis operating under the GTR + I + Γ model of nucleotide substitution, gave identical solutions and placed P. ornatus at the base of the poecilostome families, in apposition to the mytilicolid taxa. The recently suggested assignment to the Siphonostomatoida on the basis of a tubular mouth cone in the pygmy male was rejected not only by the molecular data but also by new morphological observations. Scanning electron microscopy revealed that the appendage previously interpreted as the mandible was in reality the maxilla, the presumptive ‘labium’ only an intermaxillary outgrowth of the ventral cephalic sclerite bearing the widely separated paragnaths, and that there was no basal fusion between the labrum and the ‘posterior lip’ as in genuine siphonostomatoids. Absence of mandibles and their functional replacement by the anteriorly displaced maxillae is a unique and robust apomorphy for the Mytilicolidae and placed unequivocally P. ornatus in that family. The morphology of male Pectenophilus probably evolved as a result of global progenesis, involving early sexual maturation at the metanauplius stage and the complete cessation of somite and limb development. The molecular data were also employed to examine the relationships of two other highly modified parasitic families, the Xarifiidae (inhabiting hard corals) and the Chondracanthidae (parasitic on marine demersal fishes). Our analyses rejected the previously proposed relationship between Xarifiidae and Vahiniidae and strongly supported an Anchimolgidae + (Rhynchomolgidae + Xarifiidae) clade as sister group to the Sabelliphilidae within a monophyletic Lichomolgoidea. The obtained topology suggests that the common ancestor of this clade had already established a symbiotic relationship with scleractinian corals and that host switching occurred only secondarily in the Rhynchomolgidae, involving predominantly other cnidarian and occasionally noncnidarian hosts. Reassessment of the morphology of Parangium provided new evidence for a relationship with the xarifiids, rendering its current position in the Serpulidicolidae extremely unlikely. Both parsimony and Bayesian analyses revealed an unexpected but strongly supported relationship between the Chondracanthidae and Pseudanthessiidae. This result contrasts with earlier views advocating affinity to the Synapticolidae or Lichomolgidae, but was congruent with the previously unnoticed morphological similarity in antennary armature patterns in the first copepodid stage. The morphological grounds used to establish the Lernaeosoleidae were shown to be secondarily derived characters shared with one or several chondracanthid genera. Particularly the similarity between the Lernaeosoleidae and Markevitchielinus demonstrated that the former evolved from a mesoparasitic ancestor within the Chondracanthidae and consequently should sink as a synonym of the latter. © 2006 The Linnean Society of London, Biological Journal of the Linnean Society, 2006, 87 , 403–425.     

Comparative floral structure and systematics in Celastrales (Celastraceae, Parnassiaceae, Lepidobotryaceae)

Floral morphology, anatomy and histology in the newly circumscribed order Celastrales, comprising Celastraceae, Parnassiaceae and Lepidobotryaceae are studied comparatively. Several genera of Celastraceae and Lepidobotrys (Lepidobotryaceae) were studied for the first time in this respect. Celastraceae are well supported as a group by floral structure (including genera that were in separate families in earlier classifications); they have dorsally bulged‐up locules (and thus apical septa) and contain oxalate druses in their floral tissues. The group of Celastraceae and Parnassiaceae is also well supported. They share completely syncarpous gynoecia with commissural stigmatic lobes (and strong concomitant development of the commissural vascular bundles but weak median carpel bundles), only weakly crassinucellar or incompletely tenuinucellar ovules with an endothelium, partly fringed sepals and petals, protandry in bisexual flowers combined with herkogamy by the movement of stamens and anther abscission, and stamens fused with the ovary. In contrast, Lepidobotryaceae are more distant from the other two families, sharing only a handful of features with Celastraceae (not Parnassiaceae), such as pseudohermaphroditic flowers, united stamen bases forming a collar around the gynoecium and seeds with a conspicuous aril. However, all three families together are also somewhat supported as a group and share petals that are not retarded in late floral bud development, 3‐carpellate gynoecia, ventral slits of carpels closed by long interlocking epidermal cells and pollen tube transmitting tissue encompassing several cell layers, both integuments usually more than two cell layers thick, and only weak or lacking floral indumentum. In some molecular analyses Celastrales form an unsupported clade with Malpighiales and Oxalidales. This association is supported by floral structure, especially between Celastrales and Malpighiales. Among Celastrales, Lepidobotryaceae especially share special features with Malpighiales, including a diplostemonous androecium with ten fertile stamens, epitropous ovules with an obturator and strong vascularization around the chalaza. © 2005 The Linnean Society of London, Botanical Journal of the Linnean Society, 2005, 149 , 129–194.     

Do tracheid microstructure and the presence of minute crystals link Nymphaeaceae,Cabombaceae and Hydatellaceae?

Original scanning electron microscopy (SEM) observations are presented for stems of Brasenia schreberi and Cabomba caroliniana of Cabombaceae and three species of Trithuria of Hydatellaceae. End walls of stem tracheids of Brasenia have the same peculiar microstructure that we have reported in Barclaya, Euryale, Nuphar, Nymphaea (including Ondinea) and Victoria of Nymphaeaceae. This feature unites Cabombaceae with Nymphaeaceae. The minute rhomboidal crystals on the surfaces of stellate parenchyma cells of Brasenia reported by Solereder (1906. Oxford: University Press), but not noticed since, are figured. They are like the minute crystals of the often‐mentioned astrosclereids of Nymphaeaceae. Neither of these two features has been observed in Hydatellaceae. If the absence of these two features can be confirmed, the reason may be more related to ecology, development, habit and anatomical organization than to degree of phylogenetic relationship as shown by molecular studies. Anatomical observations on the stem anatomy of Trithuria are offered on the basis of paraffin sections prepared for a paper by Cheadle & Kosakai (1975. American Journal of Botany 62: 1017–1026); that study is notable for a discrepancy between an illustration of a specialized vessel element on the one hand and tabular data indicating long scalariform perforation plates on the other. Long scalariform perforation plates are mostly found in scalariformly pitted vessels of monocots, whereas the tracheary elements of Trithuria mostly have helical or annular thickenings. We were unable to demonstrate the presence of vessels in Hydatellaceae. © 2009 The Linnean Society of London, Botanical Journal of the Linnean Society, 2009, 159 , 572–582.     

The Rubiaceae of Angola

A treatment of the Rubiaceae of Angola is presented based on herbarium collections kept at BM, BR, COI, K, LISC, LISU, LUA, LUAI, P, and PRE. The basionyms, relevant synonyms, and types from Angola are cited. For each taxon, one collection is cited for each province. An exsiccata list with over 3300 collections examined and identified during this work is provided. There are 108 genera, 422 species, and 40 infraspecific taxa of Rubiaceae in Angola. Fourteen genera and 126 species and infraspecific taxa are restricted to Cabinda. The rate of endemism of the family is c. 19%, with 86 taxa endemic to Angola (16 of which are restricted to Cabinda). Two genera are endemic. A new subspecies and a new variety are described. There are 21 unnamed entities requiring further research. © 2008 The Linnean Society of London, Botanical Journal of the Linnean Society , 2008, 156 , 537–638.     

The Piltdown forgery: a re-statement of the case against Hinton

A review of the evidence supports the conclusion reached by Gardiner and Currant in 1996 that the hoaxer was Martin Hinton, who worked in the Geology and Zoology Departments of the Natural History Museum throughout the Piltdown affair. This was based primarily on the discovery in 1978 of a cabin trunk in the loft space immediately above what had been the office of the Keeper of Zoology − which post Hinton occupied between 1936 and 1945. This contained material similarly stained to that discovered at Piltdown, while several of the pieces had also been whittled in an identical fashion to the last find at Piltdown – the notorious 'cricket bat'. Additional proof came from Hinton's executor who discovered eight human teeth varyingly stained in a tobacco tin of Hinton's. These revealed that the forger used two methods for staining his material, one of which involved decalcification, a process which converted apatite into gypsum, the other of which did not. The material in the trunk was stained using the first method, the teeth obtained from his executor, the second. The analyses of the contents of the trunk (carried out in 1995−6) and of the tobacco tin (1997−8) are reported for the first time.  © 2003 The Linnean Society of London, Zoological Journal of the Linnean Society, 2003, 139 , 315−335.     

Molecular evidence using enzyme and RAPD markers for sympatric evolution in British species of Tetramesa (Hymenoptera: Eurytomidae)

Some species of the insect genus Tetramesa (Hymenoptera: Eurytomidae), which has a world‐wide distribution, are morphologically very similar, both in the adult and larval stages. In the British Isles, there are 37 recorded species, all of which feed on grasses as larvae and are largely host specific. Some form galls on their hosts; others do not. We used a range of enzyme and random amplified polymorphic DNA (RAPD) markers to investigate a complex of five cryptic species occurring sympatrically in the UK, collected from seven sites in mainland England and Wales: T. calamagrostidis (von Schlechtendal), T. longicornis (Walker) and T. petiolata (Walker) infesting different grass hosts, and T. hyalipennis (Walker) s.l. comprising two‐host adapted forms (labelled 1 and 2) reared from the grasses Elymus repens and E. farctus, respectively. Nine soluble enzyme systems (some known to be polymorphic in other insects) and 37 RAPD primers allowed taxonomic separation of the species. However, whilst RAPD markers were able to discriminate between the two host‐adapted forms of T. hyalipennis, enzyme markers (producing phenotypic profiles in the absence of genetic crosses) could not. Upon calculating genetic distances for the RAPD data from which a cladogram of Euclidean distances (relatedness) was produced along with multivariate analysis of the data, T. longicornis was shown to be the most ‘basal’ species, and most related to T. hyalipennis s.l.; T. calamagrostidis and T. petiolata were found to be more distantly related to these species but most closely related to each other. The two forms of T. hyalipennis s.l. appear to be the most closely related of any of the species investigated, probably diverging the most recently. From this data, and since the populations examined were all sympatric without obvious physical barriers to reproduction, it can be concluded that some degree of sympatric evolution has occurred, most obviously in the case of the host‐adapted forms of T. hyalipennis. If so, this complex of species could be another rare example of sympatric speciation in insects. Further research using more sophisticated molecular markers such as microsatellites, amplified fragment length polymorphic markers (AFLPs) and DNA sequencing (e.g. of mtDNA and ribosomal DNA regions), in conjunction with behavioural studies, are required to further elucidate this interesting species group. © 2004 The Linnean Society of London, Biological Journal of the Linnean Society, 2004, 83 , 509–525.